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Li, V. FTL Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/5602 (accessed on 21 September 2026).
Li V. FTL Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/5602. Accessed September 21, 2026.
Li, Vivi. "FTL Gene" Encyclopedia, https://encyclopedia.pub/entry/5602 (accessed September 21, 2026).
Li, V. (2020, December 25). FTL Gene. In Encyclopedia. https://encyclopedia.pub/entry/5602
Li, Vivi. "FTL Gene." Encyclopedia. Web. 25 December, 2020.
FTL Gene
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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/ftl

Ferritin light chain

genes

References

  1. Burn J, Chinnery PF. Neuroferritinopathy. Semin Pediatr Neurol. 2006Sep;13(3):176-81.
  2. Cazzola M. Role of ferritin and ferroportin genes in unexplainedhyperferritinaemia. Best Pract Res Clin Haematol. 2005 Jun;18(2):251-63. Review.
  3. Craig JE, Clark JB, McLeod JL, Kirkland MA, Grant G, Elder JE, Toohey MG,Kowal L, Savoia HF, Chen C, Roberts S, Wirth MG, Mackey DA. Hereditaryhyperferritinemia-cataract syndrome: prevalence, lens morphology, spectrum ofmutations, and clinical presentations. Arch Ophthalmol. 2003 Dec;121(12):1753-61.
  4. Crompton DE, Chinnery PF, Fey C, Curtis AR, Morris CM, Kierstan J, Burt A,Young F, Coulthard A, Curtis A, Ince PG, Bates D, Jackson MJ, Burn J.Neuroferritinopathy: a window on the role of iron in neurodegeneration. BloodCells Mol Dis. 2002 Nov-Dec;29(3):522-31.
  5. Curtis AR, Fey C, Morris CM, Bindoff LA, Ince PG, Chinnery PF, Coulthard A,Jackson MJ, Jackson AP, McHale DP, Hay D, Barker WA, Markham AF, Bates D, Curtis A, Burn J. Mutation in the gene encoding ferritin light polypeptide causesdominant adult-onset basal ganglia disease. Nat Genet. 2001 Aug;28(4):350-4.
  6. Koorts AM, Viljoen M. Ferritin and ferritin isoforms I: Structure-functionrelationships, synthesis, degradation and secretion. Arch Physiol Biochem. 2007Feb;113(1):30-54. Review.
  7. Levi S, Cozzi A, Arosio P. Neuroferritinopathy: a neurodegenerative disorderassociated with L-ferritin mutation. Best Pract Res Clin Haematol. 2005Jun;18(2):265-76. Review.
  8. Madsen E, Gitlin JD. Copper and iron disorders of the brain. Annu RevNeurosci. 2007;30:317-37. Review.
  9. Millonig G, Muckenthaler MU, Mueller S. Hyperferritinaemia-cataract syndrome: worldwide mutations and phenotype of an increasingly diagnosed genetic disorder. Hum Genomics. 2010 Apr;4(4):250-62. Review.
  10. Vidal R, Ghetti B, Takao M, Brefel-Courbon C, Uro-Coste E, Glazier BS, SianiV, Benson MD, Calvas P, Miravalle L, Rascol O, Delisle MB. Intracellular ferritinaccumulation in neural and extraneural tissue characterizes a neurodegenerativedisease associated with a mutation in the ferritin light polypeptide gene. JNeuropathol Exp Neurol. 2004 Apr;63(4):363-80.
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Subjects: Genetics & Heredity
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register : Vivi Li
View Times: 919
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 25 Dec 2020
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